Jobs: pharmacovigilance

Job Title: Pharmacovigilance Services Associate. What are we looking for: Primary skill - English Language - P3 . Designation: Pharmacovigilance Services Associate. Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines. Your expected interactions are within your own...

Purpose of Pharmacovigilance Associate Role: The purpose of the Pharmacovigilance Associate role is to monitor and manage the safety aspects of clinical studies/post-marketing surveillance including but not limited to monitoring safety mailbox, preparation of safety management plan, setting up safety database for studies, processing & submission of...

DescriptionPurpose of Principal Medical Pharmacovigilance Scientist or Senior Medical Pharmacovigilance Scientist role is to monitor on the safety of patients participating in clinical trials and post marketing surveillance. This role involves the medical review and evaluation of adverse events, signal detection, risk management and contribution to safety...

Job Title: Pharmacovigilance Services Associate. What are we looking for: Primary skill - English Language - P3 . Designation: Pharmacovigilance Services Associate. Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines. Your expected interactions are within your own...

该职位来源于猎聘 Purpose of the Role: Purpose of Principal Medical Pharmacovigilance Scientist or Senior Medical Pharmacovigilance Scientist role is to monitor on the safety of patients participating in clinical trials and post marketing surveillance. This role involves the medical review and evaluation of adverse events, signal detection, risk...

该职位来源于猎聘 Reporting ToPharmacovigilance Manager Position description: Responsible for carrying out the PV related work according to ICH-GCP, SOPs, project specific procedures, and applicable regulatory requirements. Responsibilities:  Support to set up the related system and safety database Support the PV related work in the clinical...

该职位来源于猎聘 Participate in all stages of the clinical trial development process including: feasibility assessments;protocol design; CRF design; investigational site selection; generation of clinical study reports  Acts as Medical Monitor / Advisor for assigned trials or programmes  Exhibit and transmit the highest ethical standards in the...

BandLevel 4Job Description SummaryTo lead Patient Safety operational processes at the Country Organization ensuring compliance with Novartis global and local procedures, national and international regulations/ standards/ guidelines for vigilance of Novartis group approved, marketed and investigational products (incl. drugs, food supplements and medical...

BandLevel 4 Job Description SummaryTo lead Patient Safety operational processes at the Country Organization ensuring compliance with Novartis global and local procedures, national and international regulations/ standards/ guidelines for vigilance of Novartis group approved, marketed and investigational products (incl. drugs, food supplements and medical...

该职位来源于猎聘 岗位职责: 1、Responsible for medical evaluation of clinical trials and post-marketing drug ICSRs; 2、Responsible for writing or reviewing drug safety parts of documents such as IB, clinical trial protocol, ICF, clinical study report /summary, clinical study safety data review and summary;3、Responsible for drug safety signal...

SummaryTo lead Patient Safety operational processes at the Country Organization ensuring compliance with Novartis global and local procedures, national and international regulations/ standards/ guidelines for vigilance of Novartis group approved, marketed and investigational products (incl. drugs, food supplements and medical devices).About The RoleKey...

Product Safety ManagerCategory: Reg Affairs & Safety PharmacovigilanceLocation:Beijing, Beijing, CNDepartment: MRQ (Medical, Regulatory and Quality)Location: Beijing, ChinaThe PositionSupport the PV operational processes and local PV compliance management, ensuring compliance with NN procedures and regulatory requirements:Act as a key partner who...

该职位来源于猎聘Responsible for ensuring global regulatory reporting compliance by execution of processes and compliance with procedures for processing safety reports originating from clinical studies, literature, hotline, regulatory feedback data, social media and/or other sources for post-marketing products.Ensures timely identification of...

该职位来源于猎聘Responsible for ensuring global regulatory reporting compliance by execution of processes and compliance with procedures for processing safety reports originating from clinical studies, literature, hotline, regulatory feedback data, social media and/or other sources for post-marketing products.Ensures timely identification of...

BandLevel 4Job Description SummaryAct as the deputy of the Local Qualified Person for Pharmacovigilance in Novartis Country Organization to fulfill medical safety oversight and provide safety deliverables for assigned therapeutic areas/ products in China in full drug life-cycles.Job DescriptionMajor accountabilities:Act as Qualified Delegate of the Country...

BandLevel 5Job Description SummaryThis role acts as the liaison between Patient Safety & Pharmacovigilance (PS&PV) end users in the China country organization and technology service delivery partners. The position is responsible for enhancing Patient Safety & Pharmacovigilance business processes through the implementation of appropriate IT...

该职位来源于猎聘 工作时间:周一至周五15:00-0:00 工作地点:可全国任何城市homebase 职位一:主要负责Book in & 翻译(中译英),要求:2年以上PV经验,医药学相关专业,良好的英文能力,有Argus系统经验,Bookin经验,EDC RAVE 系统经验更加...

Job Description SummaryThis job holder is responsible for all activities related to the global case processing of Individual Case Safety Report (ICSR) information from all sources including post-marketing, clinical trials and published literature etc. in compliance with regulatory and internal company standards. This position may also include activities...

Job Description SummaryThis job holder is responsible for all activities related to the global case processing of Individual Case Safety Report (ICSR) information from all sources including post-marketing, clinical trials and published literature etc. in compliance with regulatory and internal company standards. This position may also include activities...

DescriptionSafety & PV Specialist I - Remote, ChinaSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the...